These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Solvent-dependent ultrafast internal conversion dynamics of n'-apo-beta-carotenoic-n'-acids (n = 8, 10, 12).
    Author: Stalke S, Wild DA, Lenzer T, Kopczynski M, Lohse PW, Oum K.
    Journal: Phys Chem Chem Phys; 2008 Apr 28; 10(16):2180-8. PubMed ID: 18404224.
    Abstract:
    The ultrafast internal conversion dynamics of 12'-apo-beta-carotenoic-12'-acid (12'CA), 10'-apo-beta-carotenoic-10'-acid (10'CA) and 8'-apo-beta-carotenoic-8'-acid (8'CA) have been investigated by femtosecond pump-probe spectroscopy. The three apocarotenoic acids were excited to the S(2) state with different excess energies. Time constants tau(1) for the IC process S(1)/ICT --> S(0) were measured by probing the dynamics at 390 nm (S(0) --> S(2)), 575 nm (S(1)/ICT --> S(n)), 850, 860 and 890 nm (S(2) --> S(n) and S(1)/ICT --> S(0)). In nonpolar solvents, the observed reduction of the tau(1) values with increasing conjugation length of the acids is consistent with a reduction of the energy gap between the S(1)/ICT and S(0) states. The values are in good agreement with those of the corresponding apocarotenals studied previously in our groups. In polar solvents, a pronounced reduction of tau(1) values was observed for 12'CA, however the behavior was different from that observed for the respective aldehyde 12'-apo-beta-caroten-12'-al studied previously: First, the degree of tau(1) reduction in methanol was milder for 12'CA (218 --> 55 ps) than for 12'-apo-beta-caroten-12'-al (220 --> 8 ps). Secondly, for 12'CA the plateau of solvent independent tau(1) values extended further into the mid-polar range (up to 0.5 on the Deltaf scale) than previously observed for the 12'-aldehyde. For 10'CA the polarity effect on the tau(1) values was weaker ( approximately 71 ps in n-hexane and 34 ps in methanol) and for 8'CA it disappeared completely ( approximately 24 ps averaged over all solvents). The polarity-induced reduction of tau(1) is likely due to the stabilization of an intramolecular charge transfer state in polar solvents. This S(1)/ICT state is also responsible for the stimulated emission in the near IR, which has been observed in this specific class of carotenoids with a terminal carboxyl group for the first time. The occurrence of stimulated emission in the near IR region is also consistent with the steady-state fluorescence spectra which are reported along with the absorption spectra of these species. Possible reasons for the different behavior of the apocarotenoic acids compared to the respective aldehydes are discussed.
    [Abstract] [Full Text] [Related] [New Search]